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Oner TO, Unalp A, Hiz S, Bayram E, et al. OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development. Epileptic Disord 2021 Oct 26. pii: epd.2021.1349. doi: 10.1684/epd.2021.1349.
PMID: 34704946

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